Highly efficient intramolecular Cannizzaro reaction between 1,3-distal formyl groups at the upper rim of a cone-calix[4]arene

被引:24
|
作者
Galli, Marzia [1 ,2 ]
Berrocal, Jose Augusto [1 ,2 ]
Di Stefano, Stefano [1 ,2 ]
Cacciapaglia, Roberta [1 ,2 ]
Mandolini, Luigi [1 ,2 ]
Baldini, Laura [3 ]
Casnati, Alessandro [3 ]
Ugozzoli, Franco [4 ]
机构
[1] Univ Roma La Sapienza, Dipartimento Chim, I-00185 Rome, Italy
[2] Univ Roma La Sapienza, CNR, IMC, I-00185 Rome, Italy
[3] Univ Parma, Dipartimento Chim Organ & Ind, I-43124 Parma, Italy
[4] Univ Parma, Dipartimento Chim Analit & Chim Fis, I-43124 Parma, Italy
关键词
CONE; DERIVATIVES; DINUCLEAR; MODELS;
D O I
10.1039/c2ob25458a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The 1,3-distal cone-calix[4] arene dialdehyde 1 undergoes Cannizzaro disproportionation in the presence of strong base, but its 1,2-vicinal regioisomer 3 and the analogous monoaldehyde 2 are unreactive under the same conditions. The high intramolecular reactivity of the 1,3-distal regioisomer 1 is measured and discussed in terms of Effective Molarity (EM).
引用
收藏
页码:5109 / 5112
页数:4
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